MedsFacts Reports covering SEBIVO
Directory listing ordered by most common adverse events for SEBIVO
Please choose an event type to view the corresponding MedsFacts report:
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 209 FDA reports)
MYALGIA ( 147 FDA reports)
FATIGUE ( 110 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 108 FDA reports)
MUSCULAR WEAKNESS ( 104 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 94 FDA reports)
PAIN IN EXTREMITY ( 86 FDA reports)
RHABDOMYOLYSIS ( 83 FDA reports)
VOMITING ( 81 FDA reports)
BLOOD LACTIC ACID INCREASED ( 80 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 78 FDA reports)
NAUSEA ( 78 FDA reports)
LACTIC ACIDOSIS ( 76 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 70 FDA reports)
GAIT DISTURBANCE ( 70 FDA reports)
ASTHENIA ( 61 FDA reports)
DYSPNOEA ( 57 FDA reports)
DEATH ( 55 FDA reports)
OEDEMA PERIPHERAL ( 52 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 50 FDA reports)
NEUROPATHY PERIPHERAL ( 50 FDA reports)
MYOPATHY ( 49 FDA reports)
RENAL IMPAIRMENT ( 49 FDA reports)
BLOOD UREA INCREASED ( 47 FDA reports)
GASTRITIS ( 46 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 45 FDA reports)
BLOOD URIC ACID INCREASED ( 45 FDA reports)
HYPOAESTHESIA ( 44 FDA reports)
MUSCLE ATROPHY ( 43 FDA reports)
HEPATITIS B ( 39 FDA reports)
WEIGHT DECREASED ( 37 FDA reports)
CHEST DISCOMFORT ( 36 FDA reports)
PALPITATIONS ( 36 FDA reports)
OLIGURIA ( 35 FDA reports)
ELECTROLYTE IMBALANCE ( 34 FDA reports)
PAIN ( 34 FDA reports)
HEART RATE INCREASED ( 33 FDA reports)
METABOLIC ACIDOSIS ( 33 FDA reports)
ABDOMINAL PAIN UPPER ( 32 FDA reports)
CHROMATURIA ( 32 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 32 FDA reports)
BLOOD GASES ABNORMAL ( 31 FDA reports)
BLOOD PRESSURE DECREASED ( 31 FDA reports)
HEPATITIS B DNA INCREASED ( 31 FDA reports)
CAESAREAN SECTION ( 29 FDA reports)
MULTI-ORGAN FAILURE ( 29 FDA reports)
TACHYPNOEA ( 29 FDA reports)
ACID BASE BALANCE ABNORMAL ( 28 FDA reports)
HYPOPHAGIA ( 28 FDA reports)
MYOSITIS ( 27 FDA reports)
NORMAL NEWBORN ( 27 FDA reports)
BLOOD BILIRUBIN INCREASED ( 26 FDA reports)
RENAL FAILURE ACUTE ( 26 FDA reports)
DECREASED APPETITE ( 25 FDA reports)
ABDOMINAL DISCOMFORT ( 22 FDA reports)
HEPATIC CIRRHOSIS ( 21 FDA reports)
DYSSTASIA ( 20 FDA reports)
JAUNDICE ( 20 FDA reports)
LUNG INFECTION ( 20 FDA reports)
MUSCLE INJURY ( 20 FDA reports)
ANURIA ( 19 FDA reports)
ASCITES ( 19 FDA reports)
FEELING ABNORMAL ( 19 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
MALAISE ( 18 FDA reports)
ABASIA ( 17 FDA reports)
ABDOMINAL PAIN ( 17 FDA reports)
BACK PAIN ( 17 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
SHOCK ( 17 FDA reports)
ARTHRALGIA ( 16 FDA reports)
COMA ( 16 FDA reports)
CSF PROTEIN INCREASED ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 16 FDA reports)
SLEEP DISORDER ( 16 FDA reports)
VIRAL LOAD INCREASED ( 16 FDA reports)
MUSCLE SWELLING ( 15 FDA reports)
BLOOD PH DECREASED ( 14 FDA reports)
PLEURAL EFFUSION ( 14 FDA reports)
RESPIRATORY RATE INCREASED ( 14 FDA reports)
SINUS TACHYCARDIA ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 14 FDA reports)
HYPOTENSION ( 13 FDA reports)
BEDRIDDEN ( 12 FDA reports)
COUGH ( 12 FDA reports)
FALL ( 12 FDA reports)
MUSCLE DISORDER ( 12 FDA reports)
PANCREATITIS ( 12 FDA reports)
ARRHYTHMIA ( 11 FDA reports)
COAGULOPATHY ( 11 FDA reports)
DISEASE PROGRESSION ( 11 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
ACIDOSIS ( 10 FDA reports)
CIRCULATORY COLLAPSE ( 10 FDA reports)
DRUG RESISTANCE ( 10 FDA reports)
MECHANICAL VENTILATION ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
POLYNEUROPATHY ( 10 FDA reports)
URINE KETONE BODY PRESENT ( 10 FDA reports)
ACUTE HEPATIC FAILURE ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 9 FDA reports)
BLOOD URINE PRESENT ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
JOINT SWELLING ( 9 FDA reports)
NERVE INJURY ( 9 FDA reports)
RALES ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
ABDOMINAL INFECTION ( 8 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
HYPOTONIA ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MOBILITY DECREASED ( 8 FDA reports)
MYOCARDITIS ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 7 FDA reports)
ALDOLASE ABNORMAL ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
POLYMYOSITIS ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 6 FDA reports)
AMYOTROPHY ( 6 FDA reports)
ANAESTHESIA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
MYOGLOBINURIA ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
OCULAR ICTERUS ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
URINE BILIRUBIN INCREASED ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
BASE EXCESS INCREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GROIN PAIN ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
MUSCULAR DYSTROPHY ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
SURGERY ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
FULL BLOOD COUNT INCREASED ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPERPLASIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LYMPHOCYTIC INFILTRATION ( 4 FDA reports)
MARROW HYPERPLASIA ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MYALGIA INTERCOSTAL ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
SPIDER NAEVUS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 4 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISTRIBUTIVE SHOCK ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MYOCARDIAL DEPRESSION ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROSENSORY HYPOACUSIS ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARVOVIRUS INFECTION ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
POIKILOCYTOSIS ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
TOTAL BILE ACIDS INCREASED ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALLERGIC COUGH ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ENEMA ADMINISTRATION ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
GAMMA BUTYRIC DEHYDROGENASE INCREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC VOLVULUS ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HISTONE ANTIBODY POSITIVE ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREMATURE DELIVERY ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABORTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
APOLIPOPROTEIN B INCREASED ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BIOPSY PERIPHERAL NERVE ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EXPOSURE VIA FATHER ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FOETAL MALPOSITION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE IN PREGNANCY ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IN VITRO FERTILISATION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MATERNAL DEATH DURING CHILDBIRTH ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY TEST NEGATIVE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
SPERM COUNT ABNORMAL ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPERMATOZOA MORPHOLOGY ABNORMAL ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRENDELENBURG'S SYMPTOM ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
MYALGIA ( 147 FDA reports)
FATIGUE ( 110 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 108 FDA reports)
MUSCULAR WEAKNESS ( 104 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 94 FDA reports)
PAIN IN EXTREMITY ( 86 FDA reports)
RHABDOMYOLYSIS ( 83 FDA reports)
VOMITING ( 81 FDA reports)
BLOOD LACTIC ACID INCREASED ( 80 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 78 FDA reports)
NAUSEA ( 78 FDA reports)
LACTIC ACIDOSIS ( 76 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 70 FDA reports)
GAIT DISTURBANCE ( 70 FDA reports)
ASTHENIA ( 61 FDA reports)
DYSPNOEA ( 57 FDA reports)
DEATH ( 55 FDA reports)
OEDEMA PERIPHERAL ( 52 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 50 FDA reports)
NEUROPATHY PERIPHERAL ( 50 FDA reports)
MYOPATHY ( 49 FDA reports)
RENAL IMPAIRMENT ( 49 FDA reports)
BLOOD UREA INCREASED ( 47 FDA reports)
GASTRITIS ( 46 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 45 FDA reports)
BLOOD URIC ACID INCREASED ( 45 FDA reports)
HYPOAESTHESIA ( 44 FDA reports)
MUSCLE ATROPHY ( 43 FDA reports)
HEPATITIS B ( 39 FDA reports)
WEIGHT DECREASED ( 37 FDA reports)
CHEST DISCOMFORT ( 36 FDA reports)
PALPITATIONS ( 36 FDA reports)
OLIGURIA ( 35 FDA reports)
ELECTROLYTE IMBALANCE ( 34 FDA reports)
PAIN ( 34 FDA reports)
HEART RATE INCREASED ( 33 FDA reports)
METABOLIC ACIDOSIS ( 33 FDA reports)
ABDOMINAL PAIN UPPER ( 32 FDA reports)
CHROMATURIA ( 32 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 32 FDA reports)
BLOOD GASES ABNORMAL ( 31 FDA reports)
BLOOD PRESSURE DECREASED ( 31 FDA reports)
HEPATITIS B DNA INCREASED ( 31 FDA reports)
CAESAREAN SECTION ( 29 FDA reports)
MULTI-ORGAN FAILURE ( 29 FDA reports)
TACHYPNOEA ( 29 FDA reports)
ACID BASE BALANCE ABNORMAL ( 28 FDA reports)
HYPOPHAGIA ( 28 FDA reports)
MYOSITIS ( 27 FDA reports)
NORMAL NEWBORN ( 27 FDA reports)
BLOOD BILIRUBIN INCREASED ( 26 FDA reports)
RENAL FAILURE ACUTE ( 26 FDA reports)
DECREASED APPETITE ( 25 FDA reports)
ABDOMINAL DISCOMFORT ( 22 FDA reports)
HEPATIC CIRRHOSIS ( 21 FDA reports)
DYSSTASIA ( 20 FDA reports)
JAUNDICE ( 20 FDA reports)
LUNG INFECTION ( 20 FDA reports)
MUSCLE INJURY ( 20 FDA reports)
ANURIA ( 19 FDA reports)
ASCITES ( 19 FDA reports)
FEELING ABNORMAL ( 19 FDA reports)
BLOOD CREATININE INCREASED ( 18 FDA reports)
MALAISE ( 18 FDA reports)
ABASIA ( 17 FDA reports)
ABDOMINAL PAIN ( 17 FDA reports)
BACK PAIN ( 17 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
SHOCK ( 17 FDA reports)
ARTHRALGIA ( 16 FDA reports)
COMA ( 16 FDA reports)
CSF PROTEIN INCREASED ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 16 FDA reports)
SLEEP DISORDER ( 16 FDA reports)
VIRAL LOAD INCREASED ( 16 FDA reports)
MUSCLE SWELLING ( 15 FDA reports)
BLOOD PH DECREASED ( 14 FDA reports)
PLEURAL EFFUSION ( 14 FDA reports)
RESPIRATORY RATE INCREASED ( 14 FDA reports)
SINUS TACHYCARDIA ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 14 FDA reports)
HYPOTENSION ( 13 FDA reports)
BEDRIDDEN ( 12 FDA reports)
COUGH ( 12 FDA reports)
FALL ( 12 FDA reports)
MUSCLE DISORDER ( 12 FDA reports)
PANCREATITIS ( 12 FDA reports)
ARRHYTHMIA ( 11 FDA reports)
COAGULOPATHY ( 11 FDA reports)
DISEASE PROGRESSION ( 11 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 11 FDA reports)
PYREXIA ( 11 FDA reports)
ACIDOSIS ( 10 FDA reports)
CIRCULATORY COLLAPSE ( 10 FDA reports)
DRUG RESISTANCE ( 10 FDA reports)
MECHANICAL VENTILATION ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
POLYNEUROPATHY ( 10 FDA reports)
URINE KETONE BODY PRESENT ( 10 FDA reports)
ACUTE HEPATIC FAILURE ( 9 FDA reports)
ANOREXIA ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 9 FDA reports)
BLOOD URINE PRESENT ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
JOINT SWELLING ( 9 FDA reports)
NERVE INJURY ( 9 FDA reports)
RALES ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
ABDOMINAL INFECTION ( 8 FDA reports)
ABORTION INDUCED ( 8 FDA reports)
COAGULATION FACTOR XI LEVEL DECREASED ( 8 FDA reports)
DEPRESSION ( 8 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 8 FDA reports)
HEPATITIS ( 8 FDA reports)
HYPOTONIA ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
MOBILITY DECREASED ( 8 FDA reports)
MYOCARDITIS ( 8 FDA reports)
PULMONARY OEDEMA ( 8 FDA reports)
ACUTE RESPIRATORY FAILURE ( 7 FDA reports)
ALDOLASE ABNORMAL ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
PCO2 DECREASED ( 7 FDA reports)
POLYMYOSITIS ( 7 FDA reports)
PROTEIN URINE PRESENT ( 7 FDA reports)
ALPHA HYDROXYBUTYRATE DEHYDROGENASE INCREASED ( 6 FDA reports)
AMYOTROPHY ( 6 FDA reports)
ANAESTHESIA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 6 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ABNORMAL ( 6 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 6 FDA reports)
HAEMOPTYSIS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
HEPATIC NEOPLASM ( 6 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPOALBUMINAEMIA ( 6 FDA reports)
MYOGLOBINURIA ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
NEUTROPHIL COUNT INCREASED ( 6 FDA reports)
OCULAR ICTERUS ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
URINE BILIRUBIN INCREASED ( 6 FDA reports)
URINE OUTPUT DECREASED ( 6 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
AREFLEXIA ( 5 FDA reports)
BASE EXCESS INCREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
CARDIOPULMONARY FAILURE ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
GASTROINTESTINAL DISORDER ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
GROIN PAIN ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 5 FDA reports)
MUSCULAR DYSTROPHY ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
RESPIRATORY ALKALOSIS ( 5 FDA reports)
SURGERY ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ABDOMINAL REBOUND TENDERNESS ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 4 FDA reports)
ACUTE ABDOMEN ( 4 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 4 FDA reports)
ASTERIXIS ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIOMEGALY ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
COMA HEPATIC ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
ENDOTRACHEAL INTUBATION ( 4 FDA reports)
ESCHERICHIA SEPSIS ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
FULL BLOOD COUNT INCREASED ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HAEMOGLOBIN INCREASED ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPERPLASIA ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
INJECTION SITE SWELLING ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LOCALISED OEDEMA ( 4 FDA reports)
LYMPHOCYTIC INFILTRATION ( 4 FDA reports)
MARROW HYPERPLASIA ( 4 FDA reports)
MOOD ALTERED ( 4 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 4 FDA reports)
MYALGIA INTERCOSTAL ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PERITONITIS BACTERIAL ( 4 FDA reports)
PO2 INCREASED ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PROCTALGIA ( 4 FDA reports)
PULMONARY HYPERTENSION ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
SPIDER NAEVUS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VITAL FUNCTIONS ABNORMAL ( 4 FDA reports)
ABNORMAL FAECES ( 3 FDA reports)
ABORTION SPONTANEOUS ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
APPENDICITIS ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ATRIAL SEPTAL DEFECT ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ABNORMAL ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CARDIAC ENZYMES INCREASED ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CHOLECYSTITIS CHRONIC ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CLAUSTROPHOBIA ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COMPLETED SUICIDE ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISTRIBUTIVE SHOCK ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
FAECES HARD ( 3 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
GALLBLADDER POLYP ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
HYPERREFLEXIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 3 FDA reports)
INTESTINAL OPERATION ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
LIMB DISCOMFORT ( 3 FDA reports)
LIVER TRANSPLANT REJECTION ( 3 FDA reports)
MARASMUS ( 3 FDA reports)
MYOCARDIAL DEPRESSION ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROSENSORY HYPOACUSIS ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARVOVIRUS INFECTION ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIPHERAL NERVE INJURY ( 3 FDA reports)
POIKILOCYTOSIS ( 3 FDA reports)
PREMATURE LABOUR ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
RHEUMATOID FACTOR INCREASED ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 3 FDA reports)
TOTAL BILE ACIDS INCREASED ( 3 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 3 FDA reports)
ACINETOBACTER INFECTION ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
ALLERGIC COUGH ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANTI-HBC ANTIBODY POSITIVE ( 2 FDA reports)
ANTI-HBE ANTIBODY POSITIVE ( 2 FDA reports)
ARTERIAL THROMBOSIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BIOPSY MUSCLE ABNORMAL ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CYANOSIS NEONATAL ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
EFFUSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ENEMA ADMINISTRATION ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 2 FDA reports)
EYELID FUNCTION DISORDER ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FOOD AVERSION ( 2 FDA reports)
GAMMA BUTYRIC DEHYDROGENASE INCREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC VOLVULUS ( 2 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 2 FDA reports)
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HEAD CIRCUMFERENCE ABNORMAL ( 2 FDA reports)
HEPATIC INFECTION ( 2 FDA reports)
HEPATITIS B ANTIGEN POSITIVE ( 2 FDA reports)
HEPATITIS B DNA ASSAY POSITIVE ( 2 FDA reports)
HEPATITIS B SURFACE ANTIGEN ( 2 FDA reports)
HEPATITIS VIRAL ( 2 FDA reports)
HISTONE ANTIBODY POSITIVE ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
JUGULAR VEIN DISTENSION ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MITOCHONDRIAL TOXICITY ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
NAIL DISCOLOURATION ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PORTAL HYPERTENSION ( 2 FDA reports)
PRE-ECLAMPSIA ( 2 FDA reports)
PREMATURE DELIVERY ( 2 FDA reports)
PROSTATIC DISORDER ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN BURNING SENSATION ( 2 FDA reports)
SMOOTH MUSCLE ANTIBODY POSITIVE ( 2 FDA reports)
SPINAL CORD DISORDER ( 2 FDA reports)
SPLEEN DISORDER ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STRESS ULCER ( 2 FDA reports)
SUDDEN CARDIAC DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYPHILIS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TROPONIN I INCREASED ( 2 FDA reports)
ULTRASOUND LIVER ABNORMAL ( 2 FDA reports)
UMBILICAL CORD ABNORMALITY ( 2 FDA reports)
UTERINE HAEMORRHAGE ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VITH NERVE PARALYSIS ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABORTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOGENITAL WARTS ( 1 FDA reports)
ANTI-HBC IGG ANTIBODY POSITIVE ( 1 FDA reports)
APOLIPOPROTEIN B INCREASED ( 1 FDA reports)
ARTERIAL CATHETERISATION ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BILE DUCT STENT INSERTION ( 1 FDA reports)
BIOPSY PERIPHERAL NERVE ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD HIV RNA INCREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BURKHOLDERIA CEPACIA COMPLEX INFECTION ( 1 FDA reports)
BURKHOLDERIA CEPACIA INFECTION ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC DISCOMFORT ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHORIA ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EXPOSURE VIA FATHER ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FOETAL MALPOSITION ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMANGIOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE IN PREGNANCY ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS B ANTIBODY POSITIVE ( 1 FDA reports)
HEPATITIS B E ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS C ANTIBODY POSITIVE ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERLACTACIDAEMIA ( 1 FDA reports)
HYPOHIDROSIS ( 1 FDA reports)
IGA NEPHROPATHY ( 1 FDA reports)
IN VITRO FERTILISATION ( 1 FDA reports)
INDIFFERENCE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LARGE FOR DATES BABY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MATERNAL DEATH DURING CHILDBIRTH ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MITOCHONDRIAL CYTOPATHY ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NAIL DYSTROPHY ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVE CONDUCTION STUDIES ABNORMAL ( 1 FDA reports)
NERVE DEGENERATION ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERIPHERAL NERVE LESION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
POISONING ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREGNANCY TEST NEGATIVE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SOMATOSENSORY EVOKED POTENTIALS ABNORMAL ( 1 FDA reports)
SPERM COUNT ABNORMAL ( 1 FDA reports)
SPERMATOZOA ABNORMAL ( 1 FDA reports)
SPERMATOZOA MORPHOLOGY ABNORMAL ( 1 FDA reports)
SPERMATOZOA PROGRESSIVE MOTILITY ABNORMAL ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STILLBIRTH ( 1 FDA reports)
THROMBIN TIME PROLONGED ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSAMINASES ABNORMAL ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRENDELENBURG'S SYMPTOM ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)